# FDA recall D-0895-2023

> **Strides Pharma Inc.** · Class II · drug recall initiated 2023-06-26.

## Product

Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08

## Reason for recall

Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.

## Distribution

Nationwide in the USA.

## Key facts

- **Recall number:** D-0895-2023
- **Recalling firm:** Strides Pharma Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-06-26
- **Report date:** 2023-07-12
- **Termination date:** 2024-05-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** East Brunswick, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0895-2023

## Citation

> AI Analytics. FDA recall D-0895-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0895-2023. Source: US FDA. Licensed CC0.

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